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Bajuk Bogdanović, Danica

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  • Bajuk Bogdanović, Danica (6)

Author's Bibliography

Self-limiting interactions in 2D–0D system: A case study of graphene oxide and 12-tungstophosphoric acid nanocomposite

Jovanović, Zoran; Mravik, Željko; Bajuk Bogdanović, Danica; Jovanović, Sonja; Marković, Smilja; Vujković, Milica; Kovač, Janez; Vengust, Damjan; Uskoković-Marković, Snežana; Holclajtner Antunović, Ivanka

(2020)

TY  - JOUR
AU  - Jovanović, Zoran
AU  - Mravik, Željko
AU  - Bajuk Bogdanović, Danica
AU  - Jovanović, Sonja
AU  - Marković, Smilja
AU  - Vujković, Milica
AU  - Kovač, Janez
AU  - Vengust, Damjan
AU  - Uskoković-Marković, Snežana
AU  - Holclajtner Antunović, Ivanka
PY  - 2020
UR  - http://dais.sanu.ac.rs/123456789/6882
AB  - In the present study we investigated the interaction between 12-tungstophosphoric acid (WPA) and graphene oxide (GO) in their nanocomposite by utilizing the loading of WPA as an intrinsic parameter for interaction tuning. The Fourier-transform infrared spectroscopy, temperature-programmed desorption, X-ray photoelectron spectroscopy, zeta-potential measurements, thermogravimetric analysis, X-ray diffraction, Raman spectroscopy and transmission electron microscopy methods revealed that ∼5–13 wt% of WPA represents critical loading that separates two distinct contributions to GO-WPA interaction. This was explained by the self-limiting nature of GO-WPA interaction, initially controlled by high dispersion of WPA on GO (up to 13 wt%), that is eventually overpowered by WPA-WPA interaction as loading increases. As a result, the WPA agglomerates are being formed because of which the hybrid character of the nanocomposite diminishes, i.e., the properties of independent components start to be manifested to greater extent. The obtained results provide an important framework for considering possible outcomes in other 2D-0D systems, whose interaction is relevant both from fundamental and applicative point of view. Thus, the GO/WPA nanocomposite illustrates how the interactions between the components can be used for tuning the properties of nanocomposite as a whole.
T2  - Carbon
T1  - Self-limiting interactions in 2D–0D system: A case study of graphene oxide and 12-tungstophosphoric acid nanocomposite
SP  - 166
EP  - 178
VL  - 156
DO  - 10.1016/j.carbon.2019.09.072
ER  - 
@article{
author = "Jovanović, Zoran and Mravik, Željko and Bajuk Bogdanović, Danica and Jovanović, Sonja and Marković, Smilja and Vujković, Milica and Kovač, Janez and Vengust, Damjan and Uskoković-Marković, Snežana and Holclajtner Antunović, Ivanka",
year = "2020",
url = "http://dais.sanu.ac.rs/123456789/6882",
abstract = "In the present study we investigated the interaction between 12-tungstophosphoric acid (WPA) and graphene oxide (GO) in their nanocomposite by utilizing the loading of WPA as an intrinsic parameter for interaction tuning. The Fourier-transform infrared spectroscopy, temperature-programmed desorption, X-ray photoelectron spectroscopy, zeta-potential measurements, thermogravimetric analysis, X-ray diffraction, Raman spectroscopy and transmission electron microscopy methods revealed that ∼5–13 wt% of WPA represents critical loading that separates two distinct contributions to GO-WPA interaction. This was explained by the self-limiting nature of GO-WPA interaction, initially controlled by high dispersion of WPA on GO (up to 13 wt%), that is eventually overpowered by WPA-WPA interaction as loading increases. As a result, the WPA agglomerates are being formed because of which the hybrid character of the nanocomposite diminishes, i.e., the properties of independent components start to be manifested to greater extent. The obtained results provide an important framework for considering possible outcomes in other 2D-0D systems, whose interaction is relevant both from fundamental and applicative point of view. Thus, the GO/WPA nanocomposite illustrates how the interactions between the components can be used for tuning the properties of nanocomposite as a whole.",
journal = "Carbon",
title = "Self-limiting interactions in 2D–0D system: A case study of graphene oxide and 12-tungstophosphoric acid nanocomposite",
pages = "166-178",
volume = "156",
doi = "10.1016/j.carbon.2019.09.072"
}
1
1

Surfactant-assisted microwave processing of ZnO particles: a simple way for designing the surface-to-bulk defect ratio and improving photo(electro)catalytic properties

Marković, Smilja; Stojković Simatović, Ivana; Ahmetović, Sanita; Veselinović, Ljiljana; Stojadinović, Stevan; Rac, Vladislav; Škapin, Srečo Davor; Bajuk Bogdanović, Danica; Janković Častvan, Ivona; Uskoković, Dragan

(Royal Society of Chemistry, 2019)

TY  - JOUR
AU  - Marković, Smilja
AU  - Stojković Simatović, Ivana
AU  - Ahmetović, Sanita
AU  - Veselinović, Ljiljana
AU  - Stojadinović, Stevan
AU  - Rac, Vladislav
AU  - Škapin, Srečo Davor
AU  - Bajuk Bogdanović, Danica
AU  - Janković Častvan, Ivona
AU  - Uskoković, Dragan
PY  - 2019
UR  - https://pubs.rsc.org/en/content/articlelanding/2019/ra/c9ra02553g
UR  - http://dais.sanu.ac.rs/123456789/6272
AB  - ZnO nanopowders were produced using microwave processing of a precipitate and applied as a photoanode for photoelectrochemical water splitting. Two different surfactants, cetyltrimethylammonium bromide (CTAB) as the cationic and Pluronic F127 as the non-ionic one, were employed to in situ adjust the surface-to-bulk defect ratio in the ZnO crystal structure and further to modify the photo(electro)catalytic activity of the ZnO photoanode. The crystal structure, morphological, textural, optical and photo(electro)catalytic properties of ZnO particles were studied in detail to explain the profound effects of the surfactants on the photoanode activity. The ZnO/CTAB photoanode displayed the highest photocurrent density of 27 mA g−1, compared to ZnO (10.4 mA g−1) and ZnO/F127 photoanodes (20 mA g−1) at 1.5 V vs. SCE in 0.1 M Na2SO4 under visible illumination of 90 mW cm−2. A significant shift of the overpotential toward lower values was also observed when photoanodes were illuminated. The highest shift of the overpotential, from 1.296 to 0.248 V vs. SCE, was recorded when the ZnO/CTAB photanode was illuminated. The ZnO/CTAB photoanode provides efficient charge transfer across the electrode/electrolyte interface, with a longer lifetime of photogenerated electron–hole pairs and reduced possibility of charge recombination. The photoconversion efficiency was improved from 1.4% for ZnO and 0.9% for ZnO/F127 to 4.2% for ZnO/CTAB at 0.510 mV. A simple procedure for the synthesis of ZnO particles with improved photo(electro)catalytic properties was established and it was found that even a small amount of CTAB used during processing of ZnO increases the surface-to-bulk defect ratio. Optimization of the surface-to-bulk defect ratio in ZnO materials enables increase of the absorption capacity for visible light, rendering of the recombination rate of the photogenerated pair, as well as increase of both the photocurrent density and photoconversion efficiency.
PB  - Royal Society of Chemistry
T2  - RSC Advances
T1  - Surfactant-assisted microwave processing of ZnO particles: a simple way for designing the surface-to-bulk defect ratio and improving photo(electro)catalytic properties
SP  - 17165
EP  - 17178
VL  - 9
IS  - 30
DO  - 10.1039/C9RA02553G
ER  - 
@article{
author = "Marković, Smilja and Stojković Simatović, Ivana and Ahmetović, Sanita and Veselinović, Ljiljana and Stojadinović, Stevan and Rac, Vladislav and Škapin, Srečo Davor and Bajuk Bogdanović, Danica and Janković Častvan, Ivona and Uskoković, Dragan",
year = "2019",
url = "https://pubs.rsc.org/en/content/articlelanding/2019/ra/c9ra02553g, http://dais.sanu.ac.rs/123456789/6272",
abstract = "ZnO nanopowders were produced using microwave processing of a precipitate and applied as a photoanode for photoelectrochemical water splitting. Two different surfactants, cetyltrimethylammonium bromide (CTAB) as the cationic and Pluronic F127 as the non-ionic one, were employed to in situ adjust the surface-to-bulk defect ratio in the ZnO crystal structure and further to modify the photo(electro)catalytic activity of the ZnO photoanode. The crystal structure, morphological, textural, optical and photo(electro)catalytic properties of ZnO particles were studied in detail to explain the profound effects of the surfactants on the photoanode activity. The ZnO/CTAB photoanode displayed the highest photocurrent density of 27 mA g−1, compared to ZnO (10.4 mA g−1) and ZnO/F127 photoanodes (20 mA g−1) at 1.5 V vs. SCE in 0.1 M Na2SO4 under visible illumination of 90 mW cm−2. A significant shift of the overpotential toward lower values was also observed when photoanodes were illuminated. The highest shift of the overpotential, from 1.296 to 0.248 V vs. SCE, was recorded when the ZnO/CTAB photanode was illuminated. The ZnO/CTAB photoanode provides efficient charge transfer across the electrode/electrolyte interface, with a longer lifetime of photogenerated electron–hole pairs and reduced possibility of charge recombination. The photoconversion efficiency was improved from 1.4% for ZnO and 0.9% for ZnO/F127 to 4.2% for ZnO/CTAB at 0.510 mV. A simple procedure for the synthesis of ZnO particles with improved photo(electro)catalytic properties was established and it was found that even a small amount of CTAB used during processing of ZnO increases the surface-to-bulk defect ratio. Optimization of the surface-to-bulk defect ratio in ZnO materials enables increase of the absorption capacity for visible light, rendering of the recombination rate of the photogenerated pair, as well as increase of both the photocurrent density and photoconversion efficiency.",
publisher = "Royal Society of Chemistry",
journal = "RSC Advances",
title = "Surfactant-assisted microwave processing of ZnO particles: a simple way for designing the surface-to-bulk defect ratio and improving photo(electro)catalytic properties",
pages = "17165-17178",
volume = "9",
number = "30",
doi = "10.1039/C9RA02553G"
}
1
6
4
7

Structural, photocatalytic and photoelectrochemical characteristics of ZnO nanoparticles synthesized by a glycine-nitrate process

Dojčinović, Milena; Stojković Simatović, Ivana; Marković, Smilja; Janković Častvan, Ivona; Bajuk Bogdanović, Danica; Stojadinović, Stevan; Rac, Vladislav; Nikolić, Maria Vesna

(Budapest : [s. n.], 2019)

TY  - CONF
AU  - Dojčinović, Milena
AU  - Stojković Simatović, Ivana
AU  - Marković, Smilja
AU  - Janković Častvan, Ivona
AU  - Bajuk Bogdanović, Danica
AU  - Stojadinović, Stevan
AU  - Rac, Vladislav
AU  - Nikolić, Maria Vesna
PY  - 2019
UR  - http://dais.sanu.ac.rs/123456789/6998
AB  - Zinc oxide is a semiconductor material which still, after a century of scientific research, shows great potential in modern day utilisements such as heterogenous photocatalysis of organic pollutants and as a photoanode material for efficient water splitting and oxygen generation. In this work zinc oxide was synthesized by a glycine-nitrate combustion process, which is a cheap, simple and efficient method for synthesizing transition metal oxides. The obtained powder was calcined at 400 and 500 °C and samples were characterized in detail using X-ray powder diffraction (XRPD), Fourier-trasform infrared spectroscopy (FTIR), Raman spectroscopy, field emission scanning electron microscopy (FESEM), photoluminescence spectroscopy (PL) and UV-Vis diffuse reflectance spectroscopy (DRS). Photoelectrocatalytic properties were investigated via electrochemical methods: linear voltammetry (LV), chronoamperometry (CA) and impedance spectroscopy (EIS). The results show that the obtained samples are nanocrystalline wurtzite zinc oxide with no impurities, with average particle diameters of 33 nm (annealed at 400 °C) and 48 nm (annealed at 500 °C). Both samples show significant amounts of various crystal deffects. The determined zinc oxide band gap was lower than the band gap of bulk zinc oxide. Photoelectrochemical measurements revealed that this material is photostable and reactive to light. Water oxidation is enhanced by exposing the light. Finally, photocatalytic properties were tested via determining kinetic parameters of organic pollutant decomposition. Both samples showed excellent photocatalytic activity by decomposing methylene blue and phenol.
PB  - Budapest : [s. n.]
C3  - Abstracts / International Workshop on Woman in Ceramic Science (WoCeram2019), April 7-9, 2019/ Budapest, Hungary, Novotel Danube Budapest
T1  - Structural, photocatalytic and photoelectrochemical characteristics of ZnO nanoparticles synthesized by a glycine-nitrate process
SP  - 16
EP  - 16
ER  - 
@conference{
author = "Dojčinović, Milena and Stojković Simatović, Ivana and Marković, Smilja and Janković Častvan, Ivona and Bajuk Bogdanović, Danica and Stojadinović, Stevan and Rac, Vladislav and Nikolić, Maria Vesna",
year = "2019",
url = "http://dais.sanu.ac.rs/123456789/6998",
abstract = "Zinc oxide is a semiconductor material which still, after a century of scientific research, shows great potential in modern day utilisements such as heterogenous photocatalysis of organic pollutants and as a photoanode material for efficient water splitting and oxygen generation. In this work zinc oxide was synthesized by a glycine-nitrate combustion process, which is a cheap, simple and efficient method for synthesizing transition metal oxides. The obtained powder was calcined at 400 and 500 °C and samples were characterized in detail using X-ray powder diffraction (XRPD), Fourier-trasform infrared spectroscopy (FTIR), Raman spectroscopy, field emission scanning electron microscopy (FESEM), photoluminescence spectroscopy (PL) and UV-Vis diffuse reflectance spectroscopy (DRS). Photoelectrocatalytic properties were investigated via electrochemical methods: linear voltammetry (LV), chronoamperometry (CA) and impedance spectroscopy (EIS). The results show that the obtained samples are nanocrystalline wurtzite zinc oxide with no impurities, with average particle diameters of 33 nm (annealed at 400 °C) and 48 nm (annealed at 500 °C). Both samples show significant amounts of various crystal deffects. The determined zinc oxide band gap was lower than the band gap of bulk zinc oxide. Photoelectrochemical measurements revealed that this material is photostable and reactive to light. Water oxidation is enhanced by exposing the light. Finally, photocatalytic properties were tested via determining kinetic parameters of organic pollutant decomposition. Both samples showed excellent photocatalytic activity by decomposing methylene blue and phenol.",
publisher = "Budapest : [s. n.]",
journal = "Abstracts / International Workshop on Woman in Ceramic Science (WoCeram2019), April 7-9, 2019/ Budapest, Hungary, Novotel Danube Budapest",
title = "Structural, photocatalytic and photoelectrochemical characteristics of ZnO nanoparticles synthesized by a glycine-nitrate process",
pages = "16-16"
}

Electrochemical oxidation of maricite NaFePO4 in mild aqueous solutions as a way to boost its charge storage capacity

Petrović, Tamara; Milović, Miloš; Bajuk Bogdanović, Danica; Vujković, Milica

(Belgrade : Institute of Technical Sciences of SASA, 2019)

TY  - CONF
AU  - Petrović, Tamara
AU  - Milović, Miloš
AU  - Bajuk Bogdanović, Danica
AU  - Vujković, Milica
PY  - 2019
UR  - http://dais.sanu.ac.rs/123456789/6971
AB  - Lithium has a low abundance in the Earth's crust, which in a few years will lead to difficult lithium production, and therefore difficult production of lithium-ion batteries. Sodium-ion batteries, on the other hand, have been proven to be a good replacement. The material obtained from iron combined with the phosphate and pyrophosphate compounds of sodium has attracted attention as a possible cathode material for sodium-ion batteries. NaFePO4 exists in two polymorphic structures (triphylite and maricite). Maricite NaFePO4 is a more thermodynamically stable structure than triphylite NaFePO4 but doesn’t have channels for Na+ movement and electrochemical performance of this structure is low. In comparison to maricite NaFePO4, triphylite NaFePO4 (structural analogue to LiFePO4) has one-dimensional channels for Na+-ions movement and better electrochemical activity but it is not stable and is difficult to synthesize. Herein, the maricite NaFePO4 can be obtained by sintering a polyanionic compound, Na4Fe3(PO4)2P2O7, at temperatures above 600 °C, as shown by XRD. Na4Fe3(PO4)2P2O7 is synthesized by the glycine-nitrate process after which it was sintered at temperatures above 500 °C. The glycine-nitrate process was found to catalyze the decomposition of the sintered Na4Fe3(PO4)2P2O7 to the NaFePO4 maricite. The electrochemical characterization of the sintered material, evaluated in aqueous NaNO3 and LiNO3 electrolyte by cyclic voltammetry, showed poor electrochemical activity of maricite NaFePO4. By exposing the sintered material to high anodic potentials, the electrochemical activity and specific capacity of the material were increased by 50% in case of NaNO3 and 80% in case of LiNO3 relative to the pristine with low activity. After electrochemical measurements, residual powder was characterized by FTIR and Raman spectroscopy. It was shown that high anodic polarization of the material tested in LiNO3 causes the formation of triphylite LiFePO4. Similarly, it is assumed that the electrochemical activity obtained by deep anodic polarization of the material in NaNO3 electrolyte originates from the formed triphylite NaFePO4. The obtained results open novel directions regarding the use of NaFePO4 in metal-ion rechargeable batteries.
PB  - Belgrade : Institute of Technical Sciences of SASA
C3  - Program and the Book of abstracts / Eighteenth Young Researchers' Conference Materials Sciences and Engineering, December 4-6, 2019, Belgrade, Serbia
T1  - Electrochemical oxidation of maricite NaFePO4 in mild aqueous solutions as a way to boost its charge storage capacity
SP  - 48
EP  - 48
ER  - 
@conference{
author = "Petrović, Tamara and Milović, Miloš and Bajuk Bogdanović, Danica and Vujković, Milica",
year = "2019",
url = "http://dais.sanu.ac.rs/123456789/6971",
abstract = "Lithium has a low abundance in the Earth's crust, which in a few years will lead to difficult lithium production, and therefore difficult production of lithium-ion batteries. Sodium-ion batteries, on the other hand, have been proven to be a good replacement. The material obtained from iron combined with the phosphate and pyrophosphate compounds of sodium has attracted attention as a possible cathode material for sodium-ion batteries. NaFePO4 exists in two polymorphic structures (triphylite and maricite). Maricite NaFePO4 is a more thermodynamically stable structure than triphylite NaFePO4 but doesn’t have channels for Na+ movement and electrochemical performance of this structure is low. In comparison to maricite NaFePO4, triphylite NaFePO4 (structural analogue to LiFePO4) has one-dimensional channels for Na+-ions movement and better electrochemical activity but it is not stable and is difficult to synthesize. Herein, the maricite NaFePO4 can be obtained by sintering a polyanionic compound, Na4Fe3(PO4)2P2O7, at temperatures above 600 °C, as shown by XRD. Na4Fe3(PO4)2P2O7 is synthesized by the glycine-nitrate process after which it was sintered at temperatures above 500 °C. The glycine-nitrate process was found to catalyze the decomposition of the sintered Na4Fe3(PO4)2P2O7 to the NaFePO4 maricite. The electrochemical characterization of the sintered material, evaluated in aqueous NaNO3 and LiNO3 electrolyte by cyclic voltammetry, showed poor electrochemical activity of maricite NaFePO4. By exposing the sintered material to high anodic potentials, the electrochemical activity and specific capacity of the material were increased by 50% in case of NaNO3 and 80% in case of LiNO3 relative to the pristine with low activity. After electrochemical measurements, residual powder was characterized by FTIR and Raman spectroscopy. It was shown that high anodic polarization of the material tested in LiNO3 causes the formation of triphylite LiFePO4. Similarly, it is assumed that the electrochemical activity obtained by deep anodic polarization of the material in NaNO3 electrolyte originates from the formed triphylite NaFePO4. The obtained results open novel directions regarding the use of NaFePO4 in metal-ion rechargeable batteries.",
publisher = "Belgrade : Institute of Technical Sciences of SASA",
journal = "Program and the Book of abstracts / Eighteenth Young Researchers' Conference Materials Sciences and Engineering, December 4-6, 2019, Belgrade, Serbia",
title = "Electrochemical oxidation of maricite NaFePO4 in mild aqueous solutions as a way to boost its charge storage capacity",
pages = "48-48"
}

Study of the interaction between graphene oxide and 12-tungstophosphoric acid in their nanocomposite

Mravik, Željko; Bajuk Bogdanović, Danica; Marković, Smilja; Kovač, Janez; Holclajtner Antunović, Ivanka; Jovanović, Zoran

(Belgrade : Materials Research Society of Serbia, 2018)

TY  - CONF
AU  - Mravik, Željko
AU  - Bajuk Bogdanović, Danica
AU  - Marković, Smilja
AU  - Kovač, Janez
AU  - Holclajtner Antunović, Ivanka
AU  - Jovanović, Zoran
PY  - 2018
UR  - http://dais.sanu.ac.rs/123456789/3666
AB  - The rich surface chemistry and large surface area of graphene oxide (GO) provide a platform for various functional materials that synergistically enhance charge storage properties of the composite. In present work we have investigated interaction between GO and 12- thungstophosphoric acid (WPA) in their nanocomposites as a function of different mass ratio of constituents. For this purpose, the Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectrometry (XPS), temperature programmed desorption method (TPD) and thermogravimetric/differential thermal analysis (TGA-DTA) methods were used. FTIR spectra have shown shifts and splitting of characteristic bands of WPA as a result of interactions with GO. Both XPS and TPD methods have shown an initial decrease of the total amount of surface oxygen groups of GO, with a minimum at around 10 wt.% of WPA, above which a restoration of the amount of surface oxygen groups was noticed. TGA-DTA analysis revealed an improved thermal stability of the material up to 25 wt.% of WPA; at higher loading of WPA the thermal properties of nanocomposite became alike to the ones of individual components. The obtained results suggest optimal conditions for preparation of GO-WPA nanocomposites for electrochemical charge storage applications.
PB  - Belgrade : Materials Research Society of Serbia
C3  - Programme and The Book of Abstracts / Twentieth Annual Conference YUCOMAT 2018, Herceg Novi, September 3-7, 2018
T1  - Study of the interaction between graphene oxide and 12-tungstophosphoric acid in their nanocomposite
SP  - 110
EP  - 110
ER  - 
@conference{
author = "Mravik, Željko and Bajuk Bogdanović, Danica and Marković, Smilja and Kovač, Janez and Holclajtner Antunović, Ivanka and Jovanović, Zoran",
year = "2018",
url = "http://dais.sanu.ac.rs/123456789/3666",
abstract = "The rich surface chemistry and large surface area of graphene oxide (GO) provide a platform for various functional materials that synergistically enhance charge storage properties of the composite. In present work we have investigated interaction between GO and 12- thungstophosphoric acid (WPA) in their nanocomposites as a function of different mass ratio of constituents. For this purpose, the Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectrometry (XPS), temperature programmed desorption method (TPD) and thermogravimetric/differential thermal analysis (TGA-DTA) methods were used. FTIR spectra have shown shifts and splitting of characteristic bands of WPA as a result of interactions with GO. Both XPS and TPD methods have shown an initial decrease of the total amount of surface oxygen groups of GO, with a minimum at around 10 wt.% of WPA, above which a restoration of the amount of surface oxygen groups was noticed. TGA-DTA analysis revealed an improved thermal stability of the material up to 25 wt.% of WPA; at higher loading of WPA the thermal properties of nanocomposite became alike to the ones of individual components. The obtained results suggest optimal conditions for preparation of GO-WPA nanocomposites for electrochemical charge storage applications.",
publisher = "Belgrade : Materials Research Society of Serbia",
journal = "Programme and The Book of Abstracts / Twentieth Annual Conference YUCOMAT 2018, Herceg Novi, September 3-7, 2018",
title = "Study of the interaction between graphene oxide and 12-tungstophosphoric acid in their nanocomposite",
pages = "110-110"
}

Surface chemistry, thermal stability and structural properties of graphene oxide/12-tungstophosphoric acid nanocomposite

Mravik, Željko; Bajuk Bogdanović, Danica; Marković, Smilja; Holclajtner Antunović, Ivanka; Jovanović, Zoran

(Belgrade : Institute of Technical Sciences of SASA, 2017)

TY  - CONF
AU  - Mravik, Željko
AU  - Bajuk Bogdanović, Danica
AU  - Marković, Smilja
AU  - Holclajtner Antunović, Ivanka
AU  - Jovanović, Zoran
PY  - 2017
UR  - http://dais.sanu.ac.rs/123456789/15450
AB  - In recent years the nanocomposites of graphene oxide (GO) and different inorganic and organic compounds have shown great potential for charge storage applications. In present work we have investigated the influence of 12-tungstophosphoric acid (WPA) on surface chemistry of graphene oxide and thermal stability of nanocomposite. For this purpose nanocomposites with different mass ratios of GO and WPA were prepared. The thermal stability of nanocomposites was investigated by thermogravimetric and differential thermal analysis (TGA-DTA) while changes in surface chemistry of GO and structural properties of WPA were investigated by Fourier transform infrared spectroscopy (FTIR) and temperature programmed desorption (TPD) method. The TGA-DTA measurements of composites have shown that the major mass loss, due to carbon combustion, is shifted to higher temperatures (~500 °C vs. 380 °C of pure GO). Furthermore, when the amount of WPA is higher than 25 mass percent the nanocomposites start to act like individual components, which was also confirmed by FTIR analysis. The amount of surface oxygen groups, monitored by both TPD and FTIR methods, showed ˝V˝ shaped dependence from the quantity of WPA with minimum at about 12 mass percent of WPA. At the same time, the FTIR spectra revealed the structural changes of WPA, displayed as shifting and splitting of characteristic bands of Keggin anion structure.
PB  - Belgrade : Institute of Technical Sciences of SASA
C3  - Program and the Book of Abstracts / Sixteenth Young Researchers' Conference Materials Sciences and Engineering, December 6-8, 2017, Belgrade, Serbia
T1  - Surface chemistry, thermal stability and structural properties of graphene oxide/12-tungstophosphoric acid nanocomposite
SP  - 48
EP  - 48
ER  - 
@conference{
author = "Mravik, Željko and Bajuk Bogdanović, Danica and Marković, Smilja and Holclajtner Antunović, Ivanka and Jovanović, Zoran",
year = "2017",
url = "http://dais.sanu.ac.rs/123456789/15450",
abstract = "In recent years the nanocomposites of graphene oxide (GO) and different inorganic and organic compounds have shown great potential for charge storage applications. In present work we have investigated the influence of 12-tungstophosphoric acid (WPA) on surface chemistry of graphene oxide and thermal stability of nanocomposite. For this purpose nanocomposites with different mass ratios of GO and WPA were prepared. The thermal stability of nanocomposites was investigated by thermogravimetric and differential thermal analysis (TGA-DTA) while changes in surface chemistry of GO and structural properties of WPA were investigated by Fourier transform infrared spectroscopy (FTIR) and temperature programmed desorption (TPD) method. The TGA-DTA measurements of composites have shown that the major mass loss, due to carbon combustion, is shifted to higher temperatures (~500 °C vs. 380 °C of pure GO). Furthermore, when the amount of WPA is higher than 25 mass percent the nanocomposites start to act like individual components, which was also confirmed by FTIR analysis. The amount of surface oxygen groups, monitored by both TPD and FTIR methods, showed ˝V˝ shaped dependence from the quantity of WPA with minimum at about 12 mass percent of WPA. At the same time, the FTIR spectra revealed the structural changes of WPA, displayed as shifting and splitting of characteristic bands of Keggin anion structure.",
publisher = "Belgrade : Institute of Technical Sciences of SASA",
journal = "Program and the Book of Abstracts / Sixteenth Young Researchers' Conference Materials Sciences and Engineering, December 6-8, 2017, Belgrade, Serbia",
title = "Surface chemistry, thermal stability and structural properties of graphene oxide/12-tungstophosphoric acid nanocomposite",
pages = "48-48"
}